Perrigo Company PLC recalls H.E.B Allergy Relief fexofenadine tablets after stability testing found impurity A out of specification. Consumers should check product details and contact H.E.B for guidance.
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Perrigo Company PLC is recalling H.E.B Allergy Relief fexofenadine tablets that failed stability testing for impurity A. This could pose a risk to health if the tablets degrade over time.
The tablets failed stability testing for impurity A, which means the medication could degrade over time. This degradation might lead to potential health risks if the tablets are not stored properly or used beyond their expiration date.
H.E.B Allergy Relief tablets with specific lot numbers and expiration dates are affected. People using these allergy medications for extended periods may be at higher risk.
Check for the product name 'H.E.B Allergy Relief', fexofenadine hydrochloride tablets, 24HR, 180mg. Look for specific lot numbers and expiration dates listed in the recall notice.
Identify the product by checking the lot number and expiration date on the packaging.
The recall indicates the tablets failed stability testing for impurity A, so they are not recommended for use. Contact H.E.B for further guidance.
Check the product details and contact H.E.B for instructions on what to do with the recalled tablets.
Yes, specific lot numbers like 0HE2530, 0JE2407, 1BR0462, 0FR0460, and 0LR0363 are affected and should be avoided.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0340-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0340-2022 from Perrigo. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
